2875-18-5

  • Product Name:2,3,5,6-Tetrafluoropyridine
  • Molecular Formula:C5HF4N
  • Purity:99%
  • Molecular Weight:151.063
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Product Details;

CasNo: 2875-18-5

Molecular Formula: C5HF4N

Appearance: clear colorless liquid

Factory Sells Best Quality 2,3,5,6-Tetrafluoropyridine 2875-18-5 with steady supply

  • Molecular Formula:C5HF4N
  • Molecular Weight:151.063
  • Appearance/Colour:clear colorless liquid 
  • Vapor Pressure:42.2mmHg at 25°C 
  • Refractive Index:n20/D 1.4046(lit.)  
  • Boiling Point:106 °C at 760 mmHg 
  • PKA:-10.94±0.20(Predicted) 
  • Flash Point:30.6 °C 
  • PSA:12.89000 
  • Density:1.518 g/cm3 
  • LogP:1.63800 

2,3,5,6-Tetrafluoropyridine(Cas 2875-18-5) Usage

Synthesis

Catalytic reduction of aryl chlorides, bromides and iodides is well documented, however, aryl fluorides do not readily react under these conditions, owing to the strong C-F bond and the high activation barrier to bond breaking. Work in our laboratories showed that at high temperatures, pentafluoropyridine was converted to 2,3,5,6- tetrafluoropyridine using a palladium catalyst.

Preparation

An autoclave sprayed with PTFE was charged with pentafluoropyridine (20.0 g, ?118 mmol), HBr (32.0 g, 400 mmol) and sulpholane (40 cm3) and heated at 200 ℃ for ?48 h. The mixture was added to water and extracted into ether. The ether solution was ?shown to contain pentafluoropyridine (79%) and 2,3,5,6-tetrafluoropyridine (21%) by ?comparison of their GCMS and fluorine nmr spectra with authentic samples.

InChI:InChI=1/C5H8F2O2/c1-3-9-4(8)5(2,6)7/h3H2,1-2H3

2875-18-5 Relevant articles

Mechanistic study of Ru-NHC-catalyzed hydrodefluorination of fluoropyridines: The influence of the NHC on the regioselectivity of C-F activation and chemoselectivity of C-F versus C-H bond cleavage

McKay, David,Riddlestone, Ian M.,Macgregor, Stuart A.,Mahon, Mary F.,Whittlesey, Michael K.

, p. 776 - 787 (2015)

We describe a combined experimental and ...

Dual C-F, C-H Functionalization via Photocatalysis: Access to Multifluorinated Biaryls

Senaweera, Sameera,Weaver, Jimmie D.

, p. 2520 - 2523 (2016)

Multifluorinated biaryls are challenging...

Dual Photoredox-/Palladium-Catalyzed Cross-Electrophile Couplings of Polyfluoroarenes with Aryl Halides and Triflates

Qin, Jian,Zhu, Shengqing,Chu, Lingling

supporting information, p. 2246 - 2252 (2021/04/02)

A visible-light photoredox-/Pd-catalyzed...

Photoredox/Nickel Dual-Catalyzed Reductive Cross Coupling of Aryl Halides Using an Organic Reducing Agent

Bülow, Raoul F.,Dewanji, Abhishek,Rueping, Magnus

supporting information, p. 1611 - 1617 (2020/03/13)

A successful protocol for the reductive ...

Dihydridoboranes: Selective Reagents for Hydroboration and Hydrodefluorination

Phillips, Nicholas A.,O'hanlon, James,Hooper, Thomas N.,White, Andrew J. P.,Crimmin, Mark R.

supporting information, p. 7289 - 7293 (2019/10/08)

The preparation of a new series of dihyd...

Hydrodefluorination of fluoroaromatics by isopropyl alcohol catalyzed by a ruthenium NHC complex. An unusual role of the carbene ligand

Mai, Van Hung,Nikonov, Georgii I.

, p. 7956 - 7961 (2018/05/23)

The NHC (NHC = N-heterocyclic carbene) c...

2875-18-5 Process route

Pentafluoropyridine
700-16-3

Pentafluoropyridine

3,4-difluoropyridine
82878-63-5

3,4-difluoropyridine

3,4,5-trifluoropyridine
67815-54-7

3,4,5-trifluoropyridine

2,3,4,5-tetrafluoropyridine
3512-16-1

2,3,4,5-tetrafluoropyridine

2,3,5,6-tetrafluoropyridine
2875-18-5

2,3,5,6-tetrafluoropyridine

2,3,5‐trifluoropyridine
76469-41-5

2,3,5‐trifluoropyridine

Conditions
Conditions Yield
With triethylsilane; α,α,α-trifluorotoluene; C64H68N2OP2Ru; In tetrahydrofuran; at 69.84 ℃; for 28h; Time; stereoselective reaction; Schlenk technique; Glovebox;
42 %Spectr.
22 %Spectr.
21 %Spectr.
7 %Spectr.
3 %Spectr.
With triethylsilane; α,α,α-trifluorotoluene; C64H68N2OP2Ru; In tetrahydrofuran; at 89.84 ℃; for 28h; Time; Temperature; stereoselective reaction; Schlenk technique; Glovebox;
41 %Spectr.
26 %Spectr.
20 %Spectr.
8 %Spectr.
2 %Spectr.
2,3,5,6-tetrafluoropyridin-4-yltrimethylsilan
16297-29-3

2,3,5,6-tetrafluoropyridin-4-yltrimethylsilan

2,3,5,6-tetrafluoropyridine
2875-18-5

2,3,5,6-tetrafluoropyridine

Pentafluoropyridine
700-16-3

Pentafluoropyridine

trimethylsilyl fluoride
420-56-4

trimethylsilyl fluoride

octafluoro dipyridyl-(4,4')
3511-91-9

octafluoro dipyridyl-(4,4')

Conditions
Conditions Yield
With xenon difluoride; tetramethylammonium fluoride; In dichloromethane; at -60 ℃; for 0.166667h; Title compound not separated from byproducts.;

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